Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review (Q38222347)

31 August 2017

title

Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review (English)

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Michael R. Gionfriddo

object named as

Michael R Gionfriddo

4

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Irina Bancos

object named as

Irina Bancos

3

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Gabriela Prustsky

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object named as

Gabriela Prustsky

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Larry J Prokop

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Chaitanya Undavalli

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Noor Asi

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Juan P Brito

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Claudia L Zeballos-Palacios

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Aaron L Leppin

6

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Zhen Wang

8

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Juan P Domecq

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Tarig A Elraiyah

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publication date

7 July 2014

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published in

Clinical Endocrinology

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volume

82

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issue

3

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page(s)

338-345

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Adrenal causes of hypertension: pheochromocytoma and primary aldosteronism

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cites work

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An update on the genetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes.

21 January 2018

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Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?

21 January 2018

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Germ-line mutations in nonsyndromic pheochromocytoma

21 January 2018

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Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement

21 January 2018

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Genetics of pheochromocytoma and paraganglioma in Spanish patients.

21 January 2018

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Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites

21 January 2018

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Genetic testing in pheochromocytoma or functional paraganglioma

21 January 2018

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The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

21 January 2018

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MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

21 January 2018

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Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene

21 January 2018

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Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma

21 January 2018

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An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

21 January 2018

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A systematic review of individual patient data meta-analyses on surgical interventions

21 January 2018

1 reference

Circumstances of discovery of phaeochromocytoma: a retrospective study of 41 consecutive patients.

21 January 2018

1 reference

Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?

21 January 2018

1 reference

Phaeochromocytoma, new genes and screening strategies

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/CEN.12530

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31 August 2017

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